A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178199



Internal ID20745239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11194901..11199000hg38UCSC Ensembl
chr11:11216448..11220547hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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